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新生儿先天性疝在无体外膜肺氧合支持下的存活情况。

Survival in neonatal congenital hernia without extracorporeal membrane oxygenation support.

作者信息

Pusic A L, Giacomantonio M, Pippus K, Rees E, Gillis D A

机构信息

Department of Surgery, Izaak Walton Killam Hospital for Children, Halifax, Nova Scotia, Canada.

出版信息

J Pediatr Surg. 1995 Aug;30(8):1188-90. doi: 10.1016/0022-3468(95)90018-7.

Abstract

The experience with high-risk congenital diaphragmatic hernia (CDH) at an institution that does not offer extracorporeal membrane oxygenation (ECMO) was reviewed. Between January 1, 1983 and December 31, 1993, 38 children presented with Bochdalek-type CDH. Excluded were two infants with lethal cardiac anomalies and four presenting after 4 hours of age. Thus, the authors identified 32 high-risk patients. All had early respiratory distress and were intubated within 5 hours of birth. Sixteen were inborn; 16 were referred to the Izaak Walton Killam Children's Hospital (IWK) within 24 hours of birth. There were 19 males and 13 females. Three died before surgery could be attempted. Twenty-two survived, giving an overall survival rate of 69% (22 of 32). For 28 of the 32, the best preoperative postductal Pao2 (BPDPao2) was recorded. Fifteen of the 28 children had a BPDPao2 of greater than 100 mm Hg. Survival in this group was 14 of 15 (93%). Thirteen of the 28 patients had a BPDPao2 of less than 100 mm Hg. Survival in this group was 5 of 13 (38%). These survival rates are comparable to those of centers offering ECMO. BPDPao2 appears to be a useful discriminating variable.

摘要

对一家不提供体外膜肺氧合(ECMO)的机构中高危先天性膈疝(CDH)的治疗经验进行了回顾。在1983年1月1日至1993年12月31日期间,38例患儿被诊断为Bochdalek型CDH。排除2例患有致命心脏异常的婴儿以及4例出生4小时后就诊的患儿。因此,作者确定了32例高危患者。所有患儿均早期出现呼吸窘迫,并在出生后5小时内插管。16例为足月儿;16例在出生后24小时内被转诊至伊萨克·沃尔顿·基拉姆儿童医院(IWK)。其中男性19例,女性13例。3例在尝试手术前死亡。22例存活,总生存率为69%(32例中的22例)。32例中的28例记录了术前最佳导管后动脉血氧分压(BPDPao2)。28例患儿中有15例BPDPao2大于100 mmHg。该组的生存率为15例中的14例(93%)。28例患者中有13例BPDPao2小于100 mmHg。该组的生存率为13例中的5例(38%)。这些生存率与提供ECMO的中心相当。BPDPao2似乎是一个有用的鉴别变量。

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